Canonical Allele Identifier: CA1601790162
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173507874C= , CM000667.2:g.173507874C= GRCh38
NC_000005.9:g.172934877C= , CM000667.1:g.172934877C= GRCh37
NC_000005.8:g.172867483C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941238.1:n.5641+284C=
XR_941239.1:n.3602+284C=
XR_941240.1:n.5497+284C=
XR_941241.1:n.3078+284C=
XR_941242.1:n.5391+284C=
XR_941243.1:n.5568+284C=
XR_941244.1:n.2883+284C=
XR_941246.1:n.5261+284C=
XR_001743000.1:n.3529+284C=
XR_001743001.1:n.3056+284C=
XR_002956234.1:n.5200+284C=